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Details
Link-It Detail - Jax Mouse Phenotype - abnormal hearing physiology
Debug Stats
  • ### Total Build Time: 49 ms 21.741 KB
  • CONCEPT_NAME gt=1 ms Completed: 1 ms rowSize= 382 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 220 bytes
  • CONCEPT_SYNONYM gt=0 Completed: 0 ms rowSize= 186 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 578 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 2.376 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.577 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=41 ms Completed: 41 ms rowSize= 15.145 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.165 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
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Jax Mouse Phenotype (1)
abnormal hearing physiology MP:0001963
Definition (1)
any functional anomaly in the ability to perceive auditory stimuli
Synonyms (1)
"abnormal auditory physiology" EXACT
Parents (1)
img abnormal ear physiology MP:0003878
Children (5)
img tinnitus MP:0003741
img abnormal susceptibility to hearing loss MP:0006334
img impaired hearing MP:0006325
img abnormal hearing electrophysiology MP:0006335
img abnormal otoacoustic response MP:0006336
Ancestral Roots
RootRoot Plus OneDepthParent
img mammalian phenotype MP:0000001img hearing/vestibular/ear phenotype MP:00053774img abnormal ear physiology MP:0003878
Genes (214)

Species:
human : 214
Page Size
Current 25
  Page 1 of 9
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDFNB59494513deafness, autosomal recessive 59
INFERRED
HumanGRXCR1389207glutaredoxin, cysteine rich 1
INFERRED
HumanCEACAM16388551carcinoembryonic antigen-related cell adhesion molecule 16
INFERRED
HumanSLC26A5375611solute carrier family 26 (anion exchanger), member 5
INFERRED
HumanPTPRQ374462protein tyrosine phosphatase, receptor type, Q
INFERRED
HumanGJC3349149gap junction protein, gamma 3, 30.2kDa
INFERRED
HumanOTOG340990otogelin
INFERRED
HumanSH3PXD2B285590SH3 and PX domains 2B
INFERRED
HumanTMIE259236transmembrane inner ear
INFERRED
HumanSLC17A8246213solute carrier family 17 (vesicular glutamate transporter), member 8
INFERRED
HumanLHFPL5222662lipoma HMGIC fusion partner-like 5
INFERRED
HumanLRTOMT220074leucine rich transmembrane and O-methyltransferase domain containing
INFERRED
HumanCYS1192668cystin 1
INFERRED
HumanSYNE4163183spectrin repeat containing, nuclear envelope family member 4
INFERRED
HumanSTRC161497stereocilin
INFERRED
HumanOTOS150677otospiralin
INFERRED
HumanOTOA146183otoancorin
INFERRED
HumanGIPC3126326GIPC PDZ domain containing family, member 3
INFERRED
HumanLOXHD1125336lipoxygenase homology domains 1
INFERRED
HumanUSH1G124590Usher syndrome 1G (autosomal recessive)
INFERRED
HumanTMC1117531transmembrane channel-like 1
Click here to display 40 evidence detail records.
HumanNTNG284628netrin G2
INFERRED
HumanSRRM484530serine/arginine repetitive matrix 4
INFERRED
HumanSLITRK684189SLIT and NTRK-like family, member 6
INFERRED
HumanGPR9884059G protein-coupled receptor 98
INFERRED
XRefs (1)

XRef Types:
mp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
MPimg MP:0001963abnormal hearing physiology0self